NewRN Openings-HCA Florida Largo Hospital HCA Florida Largo HospitalRN Openings-HCA Florida Largo HospitalLargo, FLHCA Florida Largo Hospital's vision of being a nationally renowned academic medical center requires a research infrastructure that brings clinical research studies that match our patient portal and services provided. Whether you specialize in Neurosciences or Critical Care , HCA Florida Largo Hospital in Largo, Florida, offers an exciting opportunity to work alongside skilled professionals in state-of-the-art facilities.
Sr. Manager, Research Administration (Pre-Award) University of MiamiSr. Manager, Research Administration (Pre-Award)Coral Gables, FLCollaborates with other University groups such as Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Risk Management, sponsors and other relevant offices to ensure that sponsored research projects are managed in an efficient and effective manner consistent with UM policies and procedures, and applicable agency guidelines, laws and regulations. Supports the Executive Director and Associate Directors of Pre-Award in developing and delivering staff training on the unique requirements and complexities of corporate/industry funded clinical research and clinical trial projects.
Assoc. Director, Research Administration_Pre-Award (Special Projects) University of MiamiAssoc. Director, Research Administration_Pre-Award (Special Projects)Coral Gables, FLInteracts with other ORA personnel, Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Technology Transfer, Risk Management, and other relevant offices to ensure that research initiation is managed in an efficient and effective manner consistent with UM policies and procedures, and that applications are compliant and fiscally sound. The Associate Director of the Office of Research Administration (ORA) - Special Projects reports to the Associate Vice President for Research Administration and is responsible for providing leadership, oversight and management of ORA's mission for the Coral Gables, Rosenstiel, and Medical Campuses.
Assoc. Director, Research Administration University of MiamiAssoc. Director, Research AdministrationCoral Gables, FLInteracts with other ORA personnel, Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Technology Transfer, Risk Management, and other relevant offices to ensure that research initiation is managed in an efficient and effective manner consistent with UM policies and procedures, and that applications are compliant and fiscally sound. Director, Pre-Award Services, is integrally involved in the review and analysis of complex sponsored projects and provides research administration services to a portfolio of academic departments and research units, including acting as one of the institutional liaisons with external sponsors.
Assoc. Director, Research Administration (Pre-Award) University of MiamiAssoc. Director, Research Administration (Pre-Award)Coral Gables, FLInteracts with other ORA personnel, Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Technology Transfer, Risk Management, and other relevant offices to ensure that research initiation is managed in an efficient and effective manner consistent with UM policies and procedures, and that applications are compliant and fiscally sound. Director, Pre-Award Services, is integrally involved in the review and analysis of complex sponsored projects and provides research administration services to a portfolio of academic departments and research units, including acting as one of the institutional liaisons with external sponsors.
Sr. Manager, Research Administration (Contracts) - Hybrid University of MiamiSr. Manager, Research Administration (Contracts) - HybridCoral Gables, FLAs a leader in the Office of Research Administration (ORA), the Senior Manager, Research Administration (Contracts), is integrally involved in, and supervises a team responsible for, the review and analysis of complex sponsored project agreements and provides research administration services to a portfolio of academic departments and research units, including acting as one of the institutional liaisons with external sponsors to support the University mission. Interacts with other ORA personnel, Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Technology Transfer, Risk Management, and other relevant offices to ensure that research initiation is managed in an efficient and effective manner consistent with UM policies and procedures.
Manager, Research Administration University of MiamiManager, Research AdministrationCoral Gables, FLThe ORA Manager, Research Administration supports the research mission of the University of Miami and the goals of the Office of Research Administration (ORA) and is an integral partner in a sponsored programs administration team that manages service and provides guidance and direction to specific UM departments, schools, and Centers/Institutes on all post award administration functions, from award set up to award close-out. The Manager advises and interprets research funding awards and serves as the subject matter expert for sponsor policies and procedures and works closely with all Research Administration areas to ensure compliance with sponsor requirements while providing excellent service to principal investigators, researchers and administrators.
Sr. Manager, Research Administration University of MiamiSr. Manager, Research AdministrationCoral Gables, FLAs a leader in the Office of Research Administration (ORA), the Senior Manager, Research Administrator (Contracts), is integrally involved in, and supervises a team responsible for, the review and analysis of complex sponsored project agreements and provides research administration services to a portfolio of academic departments and research units, including acting as one of the institutional liaisons with external sponsors to support the University mission. Interacts with other ORA personnel, Principal Investigators and study teams, Compliance, IRB (Human Subject Research Office), Technology Transfer, Risk Management, and other relevant offices to ensure that research initiation is managed in an efficient and effective manner consistent with UM policies and procedures.
Clinical Research Coordinator Office of Research Tallahassee Memorial HealthCare IncClinical Research Coordinator Office of ResearchTallahassee, FLReports directly to Director/Clinical Research/OI and indirectly ("dotted line") to PI (who oversees incumbent's day-to-day activities) and department service line administrator (SLA). Tallahassee Memorial Healthcare (TMH) is a private, nonprofit community-based healthcare system that provides care to a 22-county region in North Florida and South Georgia.
Clinical Research Coordinator-Office of Research Tallahassee Memorial HealthcareClinical Research Coordinator-Office of ResearchTallahassee, FloridaFull timeReports directly to Director/Clinical Research/OI and indirectly (“dotted line”) to PI (who oversees incumbent’s day-to-day activities) and department service line administrator (SLA). WHO WE ARE & WHAT WE DO: Tallahassee Memorial Healthcare (TMH) is a private, nonprofit community-based healthcare system that provides care to a 22-county region in North Florida and South Georgia.
Clinical Research Analyst III - Clinical Research Hub University of FloridaClinical Research Analyst III - Clinical Research HubGainesville, FL$75,000–$85,000 / yearJob Description: The University of Florida Clinical Research Hub is seeking an experienced OnCore Systems Administrator / Clinical Research Team Lead to support and enhance clinical research operations through the configuration, administration, maintenance, and optimization of the OnCore Clinical Trials Management System (CTMS). Working collaboratively with clinical research staff, finance, and IT teams, you will manage protocol builds, billing compliance, reporting, system integrations (including Epic), and workload coordination for your assigned team member.
NewClinical Research Program Coordinator - Core-Ctr For Research Excel Tampa General HospitalClinical Research Program Coordinator - Core-Ctr For Research ExcelTampa, FL682187'',''true'',''682187'',''false'',''Submission for the position: Clinical Research Program Coordinator - Core-Ctr For Research Excel - (Job Number: 260002O6)'',''false'',''682187'',''false'',''true'',''Clinical Research Program Coordinator - Core-Ctr For Research Excel '',''260002O6'',''!*! 3 years experience in research administration, clinical research, or project management; independent working knowledge of Clinical trial management system, electronic health record, spreadsheet and database software is required.
Research Assistant 3 - Clinical Research University of MiamiResearch Assistant 3 - Clinical ResearchMiami, FLUHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process.
Medical Assistant (Clinical Research) Research Centers of AmericaMedical Assistant (Clinical Research)Hollywood, FLPart timeWith moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
Student Worker - Speech-Language Pathology Clinical-Research Assistant Nevada State UniversityStudent Worker - Speech-Language Pathology Clinical-Research AssistantFort Lauderdale, FLThey will support the SLP program by aiding faculty research and assisting with academic programming for department and clinical programming for the Speech-Language Pathology Clinic. We seek applicants who are passionate about working with this promising student population and collaborating with faculty and staff across departments to make a lasting impact in developing our institution and our community.
Medical Assistant – Clinical Research (Bilingual English/Spanish) - Miami, FL Syneos HealthMedical Assistant – Clinical Research (Bilingual English/Spanish) - Miami, FLMiami, FloridaWe are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Research Assistant I Research Centers of AmericaResearch Assistant IHollywood, FLPart timeWith moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
NewCORE Clinical Research Coordinator 1 - Core-Ctr For Research Excel Tampa General HospitalCORE Clinical Research Coordinator 1 - Core-Ctr For Research ExcelTampa, FLA Clinical Research Coordinator 1 (CRC 1) is a research professional who works under the guidance and supervision of their leader and is responsible for managing all day-to day activities of clinical trials, including but not limited to, recruitment, screening, enrollment of participants, obtaining informed consent, conducting study visits and performing protocol required procedures as permitted by policy and delegated by the Principal Investigator. A CRC 1 focuses on ways to ensure retention of clinical trial participants; tracks all study visits, reviews and validates the accuracy of financial reports; works with Research Finance and Regulatory to reconcile all items necessary to close out completed clinical trials according to established federal regulations and guidelines.
Emergency Medicine Research Faculty - Assistant/Associate Research Professor University of FloridaEmergency Medicine Research Faculty - Assistant/Associate Research ProfessorJacksonville, FloridaUF Health encompasses the Gainesville-based University of Florida colleges of Dentistry, Medicine, Nursing, Pharmacy, Public Health and Health Professions, and Veterinary Medicine; the UF Health Shands family of hospitals in Gainesville; UF Health Jacksonville medical center; UF Health North; an academic campus in Jacksonville that is home to the UF College of Medicine – Jacksonville and includes degree programs offered by the colleges of Nursing and Pharmacy; UF Health St. Johns in St. The successful candidate will be expected to develop a high-impact, funded research program that aligns with the department’s focus on pain management, emergency medical services/prehospital care, clinical toxicology, pharmacogenomics, asthma, precision emergency medicine, and other related fields, including partnering with clinicians in a multidisciplinary approach to conduct patient-focused, translational research.
Clinical Research Coordinator Headlands Research IncClinical Research CoordinatorLake Worth, FLAs a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
Medical Assistant (Clinical Research) CenExelMedical Assistant (Clinical Research)Hollywood, FloridaWith moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
Research Assistant I CenExelResearch Assistant IHollywood, FloridaWith moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
Sr. Clinical Research Coordinator - Oncology - Onsite (Full Time, Days) Nicklaus Children's HospitalSr. Clinical Research Coordinator - Oncology - Onsite (Full Time, Days)Miami, FLBeyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO''s and regulatory authorities. Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study.
Sr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days) Nicklaus Children's HospitalSr. Clinical Research Coordinator - Neurology - Onsite (Full Time, Days)Miami, FLBeyond administrative duties, responsibilities of a SCRC may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO''s and regulatory authorities. Under direction of the Senior Manager of Clinical Trial Operations, the Senior Clinical Research Coordinator, CTO (SCRC) works independently on complex projects/assignments and manages and conducts the day-to-day activities of a research study.
Research Assistant CTO (Full Time, Days) Nicklaus Children's HospitalResearch Assistant CTO (Full Time, Days)Miami, FLParticipates and coordinates research projects, works closely with research team in recruiting subjects to observational studies, maintains research databases, and assists in the drafting of research protocols and manuscripts. Enters data in databases, generates reports, performs data/database maintenance, performs data tracking, and performs queries.
Travel Clinical Research Coordinator Alcanza Clinical Research LLCTravel Clinical Research CoordinatorLake Mary, FLResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies; Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; o Filing SAE/Deviation reports to Sponsor and IRB as needed; o Documenting and reporting adverse events; o Reporting non-compliance to appropriate staff in timely manner; o Maintaining positive and effective communication with clients and team. Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed; Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed; Assist with training of new research assistants and coordinators; Assist with scheduling and planning for visit capacity for assigned studies; May set up, train and maintain all technology needed for studies; May assist with study recruitment, patient enrollment, and tracking as needed; May handle more complex study assignments and volumes; May participate in community outreach / education events; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned.
Clinical Research Coordinator 2 - CRANE Lab University of MiamiClinical Research Coordinator 2 - CRANE LabMiami, FLUnlike traditional therapeutic clinical trials that are primarily focused on investigational drugs, devices, and sponsor-driven regulatory activities, many CRANE Lab studies involve intensive participant engagement, behavioral assessment, lifestyle intervention delivery, patient-reported outcomes, and longitudinal participant support. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel.
Clinical Research Coord II - Pulmonary PulmonaryClinical Research Coord II - PulmonaryGainesville, Florida$53,000–$69,700 / yearThis role requires strong organizational, problem-solving, communication, and regulatory compliance skills, with the ability to manage multiple projects simultaneously while maintaining accuracy and attention to detail. Job Description: This position serves as a member of the clinical research team, coordinating and completing assigned clinical research activities under the direction of the Principal Investigator and Assistant Director of Research.
Clinical Assistant Professor of Higher Education Administration University of FloridaClinical Assistant Professor of Higher Education AdministrationGainesville, FloridaFollow us: @UF_COE (X), @uf_coe (Instagram), @university-of-florida-college-of-education (LinkedIn), and @UF.COE (Facebook) ABOUT THE UNIVERSITY: The University of Florida, founded in 1853, is a public land-grant, sea-grant and space-grant research university and one of the most academically varied universities in the nation. Cutting-edge interdisciplinary research and public scholarship—often conducted in partnership with other UF colleges, school districts and communities across the state and nation—are yielding powerful learning systems and models that are helping to transform education in today’s changing world, starting with our youngest learners.
Travel Clinical Research Coordinator Alcanza Clinical ResearchTravel Clinical Research CoordinatorLake Mary, FloridaRemoteResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Requesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies; Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; o Filing SAE/Deviation reports to Sponsor and IRB as needed; o Documenting and reporting adverse events; o Reporting non-compliance to appropriate staff in timely manner; o Maintaining positive and effective communication with clients and team. Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed; Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed; Assist with training of new research assistants and coordinators; Assist with scheduling and planning for visit capacity for assigned studies; May set up, train and maintain all technology needed for studies; May assist with study recruitment, patient enrollment, and tracking as needed; May handle more complex study assignments and volumes; May participate in community outreach / education events; Maintaining confidentiality of patients, customers and company information, and; Performing all other duties as requested or assigned.
Clinical Research Coord II - Pulmonary University of FloridaClinical Research Coord II - PulmonaryGainesville, FL$53,000–$69,700 / yearThis role requires strong organizational, problem-solving, communication, and regulatory compliance skills, with the ability to manage multiple projects simultaneously while maintaining accuracy and attention to detail. Job Description: This position serves as a member of the clinical research team, coordinating and completing assigned clinical research activities under the direction of the Principal Investigator and Assistant Director of Research.
Clinical Research Manager – UF Department of Emergency Medicine University of FloridaClinical Research Manager – UF Department of Emergency MedicineGainesville, FL$87,000–$95,000 / yearCollaborating closely with the Vice Chair of Research, Department Administration, and Principal Investigators, the Clinical Research Manager will support the full lifecycle of clinical studies, from proposal development through study initiation, execution, and closeout. This role is crucial in providing leadership and oversight of our clinical research mission, encompassing regulatory compliance, study operations, and administrative management to ensure all activities are conducted in accordance with the Federal regulations and University and Department policies.
Clinical Research Coord I Bayfront HealthClinical Research Coord ITAMPA, FloridaFull timeParticipate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal. Position Summary: Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.
Clinical Research Coord I Orlando HealthClinical Research Coord ITAMPA, FloridaFull timeParticipate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal. Position Summary: Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.
Clinical Research Coord I Florida Medical ClinicClinical Research Coord ITAMPA, FloridaFull timeParticipate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal. Position Summary: Participate in the development, coordination and implementation of research and administrative strategies essential to the management of clinical trials research.
Project Manager, Clinical Research University of MiamiProject Manager, Clinical ResearchMiami, FLCoordinate all submissions related to expanded access/compassionate use requests (single- and multi-patient) to applicable stakeholders, including but not limited to: PRMC, IRB, Office of Research Administration (ORA), other departments within University of Miami/Sylvester, ancillary committees, and U.S. Food and Drug Administration (FDA). Provide guidance to Sylvester investigators and staff related to expanded access/compassionate use requests, including but not limited to emergency use/non-emergency requests, FDA review and approval process, required committee reviews, internal workflows, etc.
Clinical Research Coordinator II RN Oncology AdventHealthClinical Research Coordinator II RN OncologyAltamonte Springs, FL$65,582.40–$108,646.85 / yearLicenses and Certifications: • Registered Nurse (RN) [Required] • Basic Life Support - CPR Cert (BLS) [Required] • Advanced Cardiac Life Support Cert (ACLS) [Preferred] • Certified Clinical Research Professional (SOCRA) (CCRP) [Preferred] • Certified Clinical Research Coordinator (CCRC) [Preferred] • Oncology Certified Nurse (OCN) [Preferred]. Schedule: Full time Shift: Day (United States of America) Address: 601 E ALTAMONTE DRIVE City: ALTAMONTE SPRINGS State: Florida Postal Code: 32701.
Clinical Research Manager - UF Department of Emergency Medicine University of FloridaClinical Research Manager - UF Department of Emergency MedicineGainesville, FL$87,000–$95,000 / yearCollaborating closely with the Vice Chair of Research, Department Administration, and Principal Investigators, you will support the full lifecycle of clinical studies, from proposal development through study initiation, execution, and closeout. Collaborate with departmental administrative staff to communicate anticipated PI effort changes tied to new study proposals, award initiations, and award closeouts.
Clinical Research Coordinator III (RN) Florida Cancer Specialists and Research InstituteClinical Research Coordinator III (RN)Bradenton, FLWe are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols.
PRN - Clinical Research RN I Research Centers of AmericaPRN - Clinical Research RN IHollywood, FLPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
Clinical Research Coordinator Headlands ResearchClinical Research CoordinatorLake Worth, FloridaAs a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
NewRegistered Nurse Clinical Research Coordinator Ascension HealthRegistered Nurse Clinical Research CoordinatorPensacola, FLLead study execution according to specific clinical protocols, providing specialized nursing care, administering test interventions, and ensuring continuity of care through collaboration with multidisciplinary providers. + Record accurate, compliant clinical care and study data into appropriate databases, systematically communicating trial findings, adverse events, and progress updates to the broader research team.
Clinical Research Nurse 2 University of MiamiClinical Research Nurse 2Miami, FLCertification and Licensing: Current Florida Registered Nurse license; Current American Heart Association (AHA) Basic Life Support (BLS) for healthcare providers Certification Oncology Nursing Society (ONS) provider card for Chemotherapy and Immunotherapy administration Certification in relevant specialty or field (i.e., oncology, clinical research, etc.) preferred. 2 performs all steps of the nursing process including assessing/screening of patients; interpreting data; planning, implementing, and evaluating care; coordinating care with other providers; and teaching the patient and family the knowledge and skills needed to manage their care and prevent complications while ensuring compliance with the research protocol.
Research Coordinator I University of FloridaResearch Coordinator IGainesville, FL$40,000–$45,000 / yearThe Department of Psychiatry spans services across adult, addiction, and child/adolescent specializations, including a freestanding psychiatric hospital, a large consult liaison service at the main UF Shands Hospital, the Florida Recovery Center operated by our Addiction Division, and multiple research centers including the Center for Addiction Research & Education and the Center for OCD and Related Disorders (COARD). The Department of Psychiatry includes a large outpatient center with various specialty clinics within (including one associated with our Center for Autism and Neurodevelopment), a very active inpatient service, psychiatry collaborative program for primary care practitioners, school consultation program, and community consultation services.
Clinical Research Coord - Corp Orlando Health VenturesClinical Research Coord - CorpOrlando, FLQualifications Education/Training Must meet one of the following: • Bachelor's degree in health-related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or • Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or • Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section). Education/Training Must meet one of the following: • Bachelor's degree in health-related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or • Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or • Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section).
NewResearch Assistant, Protocol Support Lab, Biorepository, FT, 8:00A - 4:30P Baptist Health South Florida IncResearch Assistant, Protocol Support Lab, Biorepository, FT, 8:00A - 4:30PMiami, FL$21.24–$25.70 / hourResponsibilities may include managing research databases by collecting and organizing patient data entry into several platforms, creating data collection tools, preparing study materials, ensuring quality control of data during entry into various Clinical Trial Management Systems (CTMS), and requesting tissue samples for research protocols when applicable. Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.
MCI Research Assistant, Protocol Support Laboratory, FT, 8:30A-5P Baptist Health South Florida IncMCI Research Assistant, Protocol Support Laboratory, FT, 8:30A-5PMiami, FL$21.24–$25.70 / hourResponsibilities may include managing research databases by collecting and organizing patient data entry into several platforms, creating data collection tools, preparing study materials, ensuring quality control of data during entry into various Clinical Trial Management Systems (CTMS), and requesting tissue samples for research protocols when applicable. Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorHollywood, FL$32–$36 / hourThis position focuses on research participant recruitment and consenting, delivering concierge-level service throughout the clinical trial journey, and coordinating biospecimen collection in collaboration with clinical research nursing, laboratory teams, and hospital departments. The Clinical Research Coordinator II (Non-RN) plays a key role in all aspects of clinical research, including screening and enrolling participants, coordinating their care and follow-up, and ensuring strict adherence to regulatory and protocol requirements.
Clinical Research Coord I Orlando Health Ventures l LLCClinical Research Coord ITampa, FLEducation/Training Must meet one of the following: Bachelor's degree in health-related field (i.e., Healthcare Administrative, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management); or Associate degree in related field (i.e., Healthcare Administration, Nursing, Respiratory Therapy, Health & Wellness or Health Information Management) and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section); or Graduate of an accredited allied health program and one (1) year of clinical research or healthcare experience (in addition to the requirements listed in the Experience section). - Family & Pet Support - Fertility benefits, adoption assistance, backup care for children/elders/pets, and pet insurance Qualifications Essential Functions Participate in the coordination of multi-site or large-scale clinical trials research studies conducted by a supervising principal investigator(s) in support of activities that meet objectives of assigned research protocol(s).
Clinical Research Analyst II-Clinical Trial Mgmt Specialist University of FloridaClinical Research Analyst II-Clinical Trial Mgmt SpecialistJacksonville, FL$64,000–$74,000 / yearJob Description: The Clinical Research Office (CRO) in the Office of Research Affairs (ORA), Dean's Administration, College of Medicine-Jacksonville, is seeking a Clinical Research Analyst II to work as a CTMS Specialist, to support clinical trial operations and protocol management within the University of Florida's Clinical Trials Management System (CTMS). The Clinical Research Analyst II provides technical support and guidance to study teams regarding the use of the CTMS and institutional processes, assists with coverage analysis activities, and supports workflow management to ensure timely and accurate completion of assigned tasks.